The Recall Desk

Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means the agency’s own highest classification or reported deaths or serious injuries, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

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All agenciesFDA (Food)FDA (Drugs)FDA (Devices)USDA FSISCPSCNHTSAEPA

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All categoriesFoodDrugMedical DeviceVehicleConsumer Product

Minimum severity

Any3+ (High and above)4+ (High and above)5+ (High and above)

Clear filters

17801–17807 of 17807

  • ModerateFDA (Drugs)·D-1377-2012·2012-06-20

    Ben Venue Recalls Octreotide Acetate Injection Due to Potential Low Fill Volume

    Ben Venue Laboratories is recalling Octreotide Acetate Injection vials because some may have low fill volume. The recall covers 6,515 packs distributed nationwide and in Puerto Rico.

    Product
    Octreotide Acetate Injection, 50 mcg/mL (0.05 mg/mL), 1 mL single dose vials, packaged in 10 x 1 mL single dose vials per pack, Rx only, Manufactured for: Bedford Laboratories, Bedford, OH 44146; Manufactured by: Ben Venue Laboratories, Inc., Bedford, OH 44146; NDC…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1379-2012·2012-06-20

    Physicians Total Care Recalls Arthrotec 75 Tablets Due to Broken Tablets

    Physicians Total Care is recalling specific lots of Arthrotec 75 tablets because they may contain broken tablets. The recall affects products distributed in North Carolina and Kentucky.

    Product
    Arthrotec 75 (diclofenac sodium and misoprostol) tablets, 75 mg/200 mcg, a) 30-count tablets per bottle (NDC 54868-4165-1); b) 60-count tablets per bottle (NDC 54868-4165-0); Rx only, Mfg. By: G.D. searle LLC Div Pfizer, New York, NY 10017; Repacked & distributed by: Physicians…
    Category
    Drug
    Distribution
    2 states
  • ModerateFDA (Drugs)·D-1376-2012·2012-06-20

    Ben Venue Recalls Midazolam HCl Injection Due to Potential Low Fill Volume

    Ben Venue Laboratories is recalling Midazolam HCl Injection vials because some may have low fill volume. The recall covers 11,161 packs distributed nationwide and in Puerto Rico.

    Product
    Midazolam HCl Injection, 5 mg/mL, 1 mL single use vials, packaged in 10 x 1 mL single use vials per pack, Rx only, Manufactured by: Ben Venue Laboratories, Inc., Bedford, OH 44146; Manufactured for: Bedford Laboratories, Bedford, OH 44146, NDC 55390-138-01; UPC 3 55390-138-01…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1381-2012·2012-06-20

    Endo Pharmaceuticals Recalls Endocet Tablets Due to Foreign Tablet Contamination

    Endo Pharmaceuticals is recalling specific bottles of Endocet 10 mg/650 mg tablets because some contained mixed 10 mg/325 mg tablets.

    Product
    Endocet (oxycodone and acetaminophen) tablets, USP, 10 mg/650 mg, 100-count tablets per bottle, Rx only, Manufactured for: Endo Pharmaceuticals Inc., Chadds Ford, PA, By: Novartis, Lincoln, NE 68501; NDC 60951-797-70.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1375-2012·2012-06-20

    Noven Recalls Daytrana Patches Due to Defective Delivery System

    Noven Pharmaceuticals is recalling 335,190 Daytrana patches because the delivery system may be miscalibrated or defective, affecting the ability to remove the release liner.

    Product
    Daytrana (methylphenidate) transdermal system patch, Delivers 10 mg over 9 hours (1.1 mg/hr), 1 patch per pouch (NDC 54092-552-01), packaged in 30-count patches per box (NDC 54092-552-30), Rx only, Manufactured for Shire US Inc., Wayne, PA 19087; by Noven Pharmaceuticals, Inc.…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1372-2012·2012-06-20

    Noven Recalls Daytrana Patches Due to Defective Delivery System

    Noven Pharmaceuticals is recalling 357,510 Daytrana (methylphenidate) patches because the delivery system may be miscalibrated or defective, affecting the ability to remove the release liner.

    Product
    DAYTRANA — DAYTRANA (METHYLPHENIDATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1380-2012·2012-06-20

    Quadrant Chemical Recalls Subpotent DermaZinc Spray Zinc Pyrithione Product

    Quadrant Chemical Corporation is recalling DermaZinc Spray because the product is subpotent and does not meet the labeled 0.25% zinc pyrithione level.

    Product
    DermaZinc Spray, 0.25% zinc pyritione, topical OTC, 4 fl oz bottle Distributed By: Dermallogix Partners, Inc. Scarborough, ME 04070
    Category
    Drug
    Distribution
    1 state